Murphy K R, Wilson M C, Irvin C G, Glezen L S, Marsh W R, Haslett C, Henson P M, Larsen G L
Am Rev Respir Dis. 1986 Jul;134(1):62-8. doi: 10.1164/arrd.1986.134.1.62.
The antigen-induced late asthmatic response (LAR) and subsequent heightened airways reactivity after this response have been associated with increased airways inflammation. Employing an animal model of the LAR in rabbits previously developed in our laboratory, 3 phases of experiments were performed to investigate the role of polymorphonuclear leukocytes (PML) in the LAR and heightened reactivity. In all 3 phases, airways reactivity to histamine and bronchoalveolar lavage analysis were performed 3 days before and 3 days after bronchial challenge with ragweed extract. In Phase 1, 2 groups of rabbits receiving nitrogen mustard were studied: an immune group received immune serum containing antiragweed IgE, and a control group received nonimmune serum. In Phase II, nitrogen mustard was administered to immune rabbits during aortic occlusion to allow the lungs to be exposed to nitrogen mustard while limiting exposure of the bone marrow to this drug, preventing depletion of PML. In Phase III, both an immune and a nonimmune group of rabbits received nitrogen mustard as in Phase I; however, prior to antigen challenge, they were repleted with a neutrophil-rich population of PML. In all experiments, no group of control (nonimmune) rabbits, whether depleted or repleted of PML, developed an immediate asthmatic response (IAR) or a LAR. In addition, no significant increases in lavage cells or airways reactivity occurred after ragweed challenge. In contrast, those animals receiving immune serum and nitrogen mustard developed an IAR; however, no LAR occurred, and no significant change in airways reactivity was observed. Rabbits receiving immune serum and nitrogen mustard with aortic occlusion developed an IAR and LAR, and airways reactivity increased.(ABSTRACT TRUNCATED AT 250 WORDS)
抗原诱导的迟发性哮喘反应(LAR)以及该反应后随后增强的气道反应性与气道炎症增加有关。利用我们实验室先前建立的兔LAR动物模型,进行了3个阶段的实验,以研究多形核白细胞(PML)在LAR和反应性增强中的作用。在所有3个阶段中,在豚草提取物支气管激发前3天和激发后3天进行气道对组胺的反应性及支气管肺泡灌洗分析。在第1阶段,研究了2组接受氮芥的兔:免疫组接受含抗豚草IgE的免疫血清,对照组接受非免疫血清。在第II阶段,在主动脉阻断期间给免疫兔施用氮芥,以使肺暴露于氮芥,同时限制骨髓对该药物的暴露,防止PML耗竭。在第III阶段,一组免疫兔和一组非免疫兔如在第I阶段一样接受氮芥;然而,在抗原激发前,用富含中性粒细胞的PML群体对它们进行补充。在所有实验中,无论是PML耗竭还是补充的对照组(非免疫)兔,均未出现速发性哮喘反应(IAR)或LAR。此外,豚草激发后灌洗细胞或气道反应性均未显著增加。相比之下,接受免疫血清和氮芥的动物出现了IAR;然而,未出现LAR,且未观察到气道反应性有显著变化。接受免疫血清和氮芥并进行主动脉阻断的兔出现了IAR和LAR,且气道反应性增加。(摘要截短于250字)